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FIG. 8 in Diversity, morphological phylogeny, and distribution of bats of the genus Molossus E. Geoffroy, 1805 (Chiroptera, Molossidae) in Brazil

FIG. 8. — Ventral view of skull of Molossus coibensis Allen, 1904. The arrow shows the absence of the basioccipital pits.

FIG. 6 in Diversity, morphological phylogeny, and distribution of bats of the genus Molossus E. Geoffroy, 1805 (Chiroptera, Molossidae) in Brazil

FIG. 6. — Molossus aztecus Saussure, 1860 skull: A, ventral view; B, posterior view; C, lateral view; D, frontal view. Scale bar: 1 mm.

FIG. 5. — Strict consensus tree from eight most parsimonious trees recovered for Molossus E. Geoffroy, 1805 in Diversity, morphological phylogeny, and distribution of bats of the genus Molossus E. Geoffroy, 1805 (Chiroptera, Molossidae) in Brazil

FIG. 5. — Strict consensus tree from eight most parsimonious trees recovered for Molossus E. Geoffroy, 1805. Numbers above the branches indicate Bootstrap values and bottom numbers indicate Bremer support values.

FIG. 3 in Diversity, morphological phylogeny, and distribution of bats of the genus Molossus E. Geoffroy, 1805 (Chiroptera, Molossidae) in Brazil

FIG. 3. — Principal Components Analysis plot of PC1 and PC2 based on 13 cranial and external variables of Molossus E. Geoffroy, 1805: A, females, B, males. Symbols: ■, M. pretiosus Miller, 1902; ■, M. rufus (E. Geoffroy, 1805); ▲, M. currentium Thomas, 1901; +, M. molossus (Pallas, 1766); X, M. coibensis Allen, 1904; ▲, M. aztecus Saussure, 1860;, M. sinaloae Allen, 1906; *, and Molossus sp.

FIG. 1 in Diversity, morphological phylogeny, and distribution of bats of the genus Molossus E. Geoffroy, 1805 (Chiroptera, Molossidae) in Brazil

FIG. 1. — Definition of skull measurements used in this study of Molossus E. Geoffroy, 1805. Abbreviations: see Material & Methods. Reprinted from Loureiro

FIG. 7 in Diversity, morphological phylogeny, and distribution of bats of the genus Molossus E. Geoffroy, 1805 (Chiroptera, Molossidae) in Brazil

FIG. 7. — Geographic range of Molossus aztecus Saussure, 1860 in Brazil (Gregorin et al. 2011). -, represents new records for the country, the numbers represent the localities described in Appendix 1.

FIG. 4 in Diversity, morphological phylogeny, and distribution of bats of the genus Molossus E. Geoffroy, 1805 (Chiroptera, Molossidae) in Brazil

FIG. 4. — Principal component analysis of the first two main components (PC1 and PC2) based on 13 cranial and external variables of Molossus molossus: A, males,B, females.Symbols:■, Rio de Janeiro; ▲, Ceará; ▼, Pará; +, Rio Grande do Sul; ▲, Piauí; ●, Mato Grosso do Sul; O, Minas Gerais; *, Bahia; ◆, Amazonas; ●, Paraíba;, São Paulo; ❚, Mato Grosso; x, Paraiba, ▼, Acre; ●, Piaui.

FIG. 19 in Diversity, morphological phylogeny, and distribution of bats of the genus Molossus E. Geoffroy, 1805 (Chiroptera, Molossidae) in Brazil

FIG. 19. — Geographic range of Molossus pretiosus Miller, 1902 in Brasil. The numbers represent the localities described in Appendix 1.

FIG. 17 in Diversity, morphological phylogeny, and distribution of bats of the genus Molossus E. Geoffroy, 1805 (Chiroptera, Molossidae) in Brazil

FIG. 17. — Geographic range of Molossus currentium Thomas, 1901 in Brasil: -, represents new records for the country. The numbers represent the locality described in Appendix 1.

FIG. 9 in Diversity, morphological phylogeny, and distribution of bats of the genus Molossus E. Geoffroy, 1805 (Chiroptera, Molossidae) in Brazil

FIG. 9. — Geographic range of Molossus coibensis Allen, 1904 in Brazil: -, Represents new records for the country. The numbers represent the localities described in Appendix 1.

FIG. 1 in New insights into the distribution and variation of Passiflora cerasina Annonay & Feuillet

FIG. 1. — Passiflora cerasina Annonay & Feuillet: A, young stems with yellow greenish leaves, cherry red tendrils and stipules; B, Mature leaf with two nectaries at the middle of petiole; C, D, Flowers from the Kaw mountain (same population as holotype and neotype); E, transversal section of the flower, showing the fourth inner series closing the nectary chamber; F, Flower from the Kapiri Creek (Saint Georges), an example of variation in the color of bracts and perianth; G, H, Fruits from the Plateau des Mines, near Saint Laurent du Maroni. Scale bars: 1 cm.

FIG. 3 in New molecular and morphological evidences favor a combination of Blechnum bakeri C.Chr. in Cranfillia Gasper & V.A.O.Dittrich (Blechnaceae, Polypodiopsida), thus extending the distribution of Cranfillia to Madagascar and East Africa

FIG. 3. — Spores of Cranfillia and Austroblechnum as observed with SEM: A, B, C. bakeri Vázquez Ferreira & S.Molino, comb. nov. (MA389177); C, D, C. mucronata (MA655870 & UC1615719, respectively); E, F, A. lherminieri (Bory ex Kunze) Gasper & V.A.O.Dittrich (BA57587). Thick and straight muri are visible in Cranfillia, as well as the spongy-trabecular middle layer of the perine (B and D). Smooth and micro-granulated perine ornamentation is observed in A. lherminieri. Scale bar: A, 17 µm; B, 9 µm; C, 7 µm; D, 1 µm; E, 8 µm; F, 2 µm.

FIG. 2 in New insights into the distribution and variation of Passiflora cerasina Annonay & Feuillet

FIG. 2. — Geographic distribution of P. cerasina Annonay & Feuillet from field collections and herbarium specimens.

opencc-by-4.0Dec 2020View details →

Repository: The Distribution of Frosts on Mars: Links to Present-Day Gully Activity

This repository contains: 1. Global calculated CO2 frost point temperatures (Kelvin) calculated at 1 ppd every 10 Ls using surface pressure from the online version of the Mars Climate Database (http://www-mars.lmd.jussieu.fr/mcd_python/) CO2 Frost Points 2. Local Solar Time and Season of THEMIS CO2 Frost Detections at gully locations corr_gully_detections_filenames_meta 3. Calculated CO2 frost amounts (kg/m^2) at 30S, 40S, 50S and 60S on pole-facing slopes Frost Amounts 4. Calculated CO2 frost amounts (kg/m^2) varying with lower material thermal inertia, slope azimuth, top material thermal inertia, top material thickness and surface albedo Frost Sensitivity 5. Predicted H2O frost lifetimes (hours) H2OFrost_Stability 6. Global THEMIS CO2 Frost Detections from Mars Year (MY) 26 MY26_THEMIS_CO2_Frost_Detections 7. THEMIS CO2 Frost Detections at gully locations (Harrison et al. 2015) from MYs 26 - 35 MY26_35_THEMIS_GULLY_CO2_Frost_Detections 8. H2O frost temperatures (Kelvin) at the Opportunity rover site Opportunity_H2OFrost 9. CO2 Frost detections made by Piqueux et al. (2016) using Mars Climate Sounder data Piqueux et al (2016) MCS CO2 Frost Detections 10. TES-derived data a) TES_MY26_H2OFrost_Temp_Map b) TES_MY26_H2OFrost_Temp_Seasonal 11. The seasonal variation of the CO2 frost point (Kelvin) at the Viking Lander sites Viking_Lander_Data

FIG. 2 in New molecular and morphological evidences favor a combination of Blechnum bakeri C.Chr. in Cranfillia Gasper & V.A.O.Dittrich (Blechnaceae, Polypodiopsida), thus extending the distribution of Cranfillia to Madagascar and East Africa

FIG. 2. — Morphology of sterile pinnae in Cranfillia species: A, Sterile frond of C. fullagari (K001092750); B-E, Basal pinnae morphology; B, C. opaca (US1431859); C, C. bakeri Vázquez Ferreira & S.Molino, comb. nov. (P00483198); D, C. mucronata (P01389538); E, C. nigra (K001092713). Scale bar: A, 28 mm; B, 6 mm; C, 10 mm; D, 17 mm; E, 7 mm.

FIG. 1 in New molecular and morphological evidences favor a combination of Blechnum bakeri C.Chr. in Cranfillia Gasper & V.A.O.Dittrich (Blechnaceae, Polypodiopsida), thus extending the distribution of Cranfillia to Madagascar and East Africa

FIG. 1. — Majority rule consensus phylogenetic tree for the genus Cranfillia estimated by Bayesian inference on the combined plastid DNA dataset (rbcL, rps4, rps4-trnS, trnL/trnL-trnF), with support values from the Maximum likelihood method and Bayesian inference. Unless mentioned next to the nodes, support values are bootstraps (BS) = 100 and posterior probabilities (PP) = 1. Scale bar is for branch lengths of the phylogram (substitutions/site).

opencc-by-4.0Nov 2018View details →

Figs 1–14 in New minute Drilini species significantly extend the distributions of Lolosia and Microselasia (Coleoptera: Elateridae: Agrypninae) in tropical Africa

Figs 1–14. Morphology of Lolosia species. 1–2 – L. gajduskovae sp. nov.: 1 – habitus, dorsal view; 2 – habitus, lateral view. 3–4 – L. smetkovae sp. nov.: 3 – habitus, dorsal view; 4 – habitus, lateral view. 5–6 – antenna, dorsal view: 5 – L. gajduskovae sp. nov.; 6 – L. smetkovae sp. nov. 7–10 – L. gajduskovae sp. nov.: 7 – head and pronotum, dorsal view; 8 – abdominal sternite IX, ventral view; 9 – aedeagus, dorsal view; 10 – aedeagus, lateral view. 11–14 – L. smetkovae sp. nov.: 11 – head and pronotum, dorsal view; 12 – abdominal sternite IX, ventral view; 13 – aedeagus, dorsal view; 14 – aedeagus, lateral view. Scale bars = 1.0 mm (Figs 1–4), 0.5 mm (Figs 5–7, 11), 0.2 mm (Figs 8–10, 12–14).

opencc-by-4.0Nov 2018View details →

Figs 15–27 in New minute Drilini species significantly extend the distributions of Lolosia and Microselasia (Coleoptera: Elateridae: Agrypninae) in tropical Africa

Figs 15–27. Morphology of Microselasia species. 15–16 – M. burgeoni (Pic, 1930): 15 – habitus, dorsal view; 16 – habitus, lateral view. 17–18 – M. sormovae sp. nov.: 17 – habitus, dorsal view; 18 – habitus, lateral view. 19–20 – M. burgeoni (Pic, 1930): 19 – apical antennomeres, ventral view, 20 – basal antennomeres, ventral view. 21 – M. sormovae sp. nov., antenna, dorsal view. 22–24 – M. burgeoni (Pic, 1930): 22 – head and pronotum, dorsal view; 23 – abdominal sternite IX, ventral view; 24 – aedeagus, dorsal view. 25–27 – M. sormovae sp. nov.: 25 – head and pronotum, dorsal view; 26 – abdominal sternite IX, ventral view; 27 – aedeagus, dorsal view. Scale bars = 1.0 mm (Figs 15–19), 0.5 mm (Figs 22, 25), 0.2 mm (Figs 20–21, 23–24, 26–27).

opencc-by-4.0Sep 2016View details →

Fig. 2 in New species of Scleromystax Günther, 1864 (Siluriformes: Callichthyidae) - extending the meridional distribution of genera endemic to the Atlantic Forest

Fig. 2. Lateral view of head, left side, showing the snout profile of Scleromystax reisi, holotype, MCP 49070, 49.3 mm SL (a), and S. salmacis, holotype, MCP 38388, 36.7 mm SL (b; modified from Britto & Reis, 2005: fig. 1).